TN2011000211A1 - PYRROLIDINES - Google Patents

PYRROLIDINES

Info

Publication number
TN2011000211A1
TN2011000211A1 TN2011000211A TN2011000211A TN2011000211A1 TN 2011000211 A1 TN2011000211 A1 TN 2011000211A1 TN 2011000211 A TN2011000211 A TN 2011000211A TN 2011000211 A TN2011000211 A TN 2011000211A TN 2011000211 A1 TN2011000211 A1 TN 2011000211A1
Authority
TN
Tunisia
Prior art keywords
compounds
formula
preparation
relates
pelvic pain
Prior art date
Application number
TN2011000211A
Other languages
French (fr)
Inventor
Kevin Neil Dack
James Edward John Mills
Sarah Elizabeth Skerratt
Original Assignee
Pfizer Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Pfizer Ltd filed Critical Pfizer Ltd
Publication of TN2011000211A1 publication Critical patent/TN2011000211A1/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/12Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/40Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00Drugs for disorders of the urinary system
    • A61P13/12Drugs for disorders of the urinary system of the kidneys
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P15/00Drugs for genital or sexual disorders; Contraceptives
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P5/00Drugs for disorders of the endocrine system
    • A61P5/24Drugs for disorders of the endocrine system of the sex hormones
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D207/00Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D207/02Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D207/04Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
    • C07D207/10Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D207/16Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/12Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links

Abstract

Cette invention concerne une classe de pyrrolidines de formule (I) et leurs dérivés pharmaceutiquement acceptables , leur utilisation en médecine, des compositions les contenant et des procédés pour leur préparation. Elle concerne également les intermédiaires utilisés dans la préparation de ces composés et dérivés. En particulier Les composés de formule (I) sont utiles pour le traitement d' affections à mediation par EP2 , telles que l endometriose , les fibromes uterins ( fibromymes) , la ménorragie, l 'adénomyose , les dysménorrhées primaire et secondaire (comprenant des symptomes de dyspareunie, de dyschexie et de douleur pelvienne chronique , le syndrome de douleur pelvienne chronique, la maladie renale polykystique et le syndrome d 'ovaire polykystiqueThis invention relates to a class of pyrrolidines of formula (I) and their pharmaceutically acceptable derivatives, their use in medicine, compositions containing them and processes for their preparation. It also relates to the intermediates used in the preparation of these compounds and derivatives. In particular, the compounds of formula (I) are useful for the treatment of affections mediated by EP2, such as endometriosis, uterine fibroids (fibromymes), menorrhagia, adenomyosis, primary and secondary dysmenorrhea (including symptoms). dyspareunia, dyschexia and chronic pelvic pain, chronic pelvic pain syndrome, polycystic renal disease and polycystic ovary syndrome

TN2011000211A 2008-11-10 2011-04-29 PYRROLIDINES TN2011000211A1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US11286908P 2008-11-10 2008-11-10
PCT/IB2009/054824 WO2010052625A1 (en) 2008-11-10 2009-10-30 Pyrrolidines

Publications (1)

Publication Number Publication Date
TN2011000211A1 true TN2011000211A1 (en) 2012-12-17

Family

ID=41503565

Family Applications (1)

Application Number Title Priority Date Filing Date
TN2011000211A TN2011000211A1 (en) 2008-11-10 2011-04-29 PYRROLIDINES

Country Status (31)

Country Link
US (1) US8278343B2 (en)
EP (1) EP2364296A1 (en)
JP (1) JP2012508225A (en)
KR (1) KR20110083733A (en)
CN (1) CN102209710A (en)
AP (1) AP2011005728A0 (en)
AR (1) AR074314A1 (en)
AU (1) AU2009312427B2 (en)
BR (1) BRPI0920924A2 (en)
CA (1) CA2741589A1 (en)
CL (1) CL2011001034A1 (en)
CO (1) CO6382112A2 (en)
CR (1) CR20110217A (en)
CU (1) CU20110093A7 (en)
DO (1) DOP2011000127A (en)
EA (1) EA201100549A1 (en)
EC (1) ECSP11011032A (en)
GE (1) GEP20125607B (en)
IL (1) IL212490A0 (en)
MA (1) MA32782B1 (en)
MX (1) MX2011004903A (en)
NI (1) NI201100092A (en)
NZ (1) NZ592311A (en)
PA (1) PA8848001A1 (en)
PE (1) PE20110663A1 (en)
SV (1) SV2011003896A (en)
TN (1) TN2011000211A1 (en)
TW (1) TW201022234A (en)
UY (1) UY32228A (en)
WO (1) WO2010052625A1 (en)
ZA (1) ZA201104310B (en)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AR074776A1 (en) * 2008-12-18 2011-02-09 Sanofi Aventis METHOD TO TREAT MACULAR DEGENERATION; MODULATING THE PATIENT'S IMMUNE SYSTEM
TW201326154A (en) 2011-11-28 2013-07-01 拜耳知識產權公司 Novel 2H-indazoles as EP2 receptor antagonists
WO2013176220A1 (en) * 2012-05-25 2013-11-28 国立大学法人京都大学 Regulation of circadian rhythm
CN110041269A (en) * 2019-05-16 2019-07-23 海门瑞一医药科技有限公司 A kind of preparation method of the chloro- 5- hydroxy pyrimidine of 2-
WO2022272062A1 (en) * 2021-06-24 2022-12-29 Reservoir Neuroscience, Inc. Ep2 antagonist compounds

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA2078790C (en) * 1991-01-21 1998-10-06 Susumu Kamata 3-benzylidene-1-carbamoyl-2-pyrrolidone analogues
AU2002358772B2 (en) * 2001-12-20 2008-11-20 Merck Serono Sa Pyrrolidine derivatives as prostaglandin modulators
WO2007005176A1 (en) * 2005-06-29 2007-01-11 Allergan, Inc. Pyrrolidinones for the treatment of glaucoma and ocular hypertension
US7592364B2 (en) * 2006-02-28 2009-09-22 Allergan, Inc. Substituted gamma lactams as therapeutic agents
US7550448B2 (en) * 2006-05-24 2009-06-23 Allergan, Inc. Therapeutic compounds
DE102006039912A1 (en) * 2006-08-25 2008-03-20 Bayer Healthcare Ag Substituted spirotetronic acids and their use
EA200901381A1 (en) * 2007-05-10 2010-06-30 Пфайзер Лимитед AZETIDINE DERIVATIVES AND THEIR APPLICATION AS ANTAGONISTS OF PROSTAGLANDIN E2

Also Published As

Publication number Publication date
EA201100549A1 (en) 2011-12-30
GEP20125607B (en) 2012-08-10
AU2009312427A1 (en) 2010-05-14
BRPI0920924A2 (en) 2016-10-04
PA8848001A1 (en) 2010-06-28
US20100120793A1 (en) 2010-05-13
KR20110083733A (en) 2011-07-20
CA2741589A1 (en) 2010-05-14
CL2011001034A1 (en) 2011-11-11
UY32228A (en) 2010-06-30
MX2011004903A (en) 2011-05-30
US8278343B2 (en) 2012-10-02
CR20110217A (en) 2011-05-12
ECSP11011032A (en) 2011-06-30
CU20110093A7 (en) 2012-01-31
NI201100092A (en) 2011-10-31
AR074314A1 (en) 2011-01-05
CO6382112A2 (en) 2012-02-15
NZ592311A (en) 2012-12-21
DOP2011000127A (en) 2011-07-15
ZA201104310B (en) 2012-02-29
PE20110663A1 (en) 2011-09-23
EP2364296A1 (en) 2011-09-14
MA32782B1 (en) 2011-11-01
IL212490A0 (en) 2011-06-30
CN102209710A (en) 2011-10-05
JP2012508225A (en) 2012-04-05
AP2011005728A0 (en) 2011-06-30
WO2010052625A1 (en) 2010-05-14
AU2009312427B2 (en) 2011-10-20
TW201022234A (en) 2010-06-16
SV2011003896A (en) 2011-07-05

Similar Documents

Publication Publication Date Title
TN2011000211A1 (en) PYRROLIDINES
MA30696B1 (en) (3-AMINO-1,2,3,4-TETRAHYDRO-9H-CARBAZOL-9-YL) -ACETIC DERIVATIVES
TN2009000450A1 (en) PYRIDINE DERIVATIVES
MA29335B1 (en) N- (N-SULFONYLAMINOMETHYL) CYCLOPROPANECARBOXAMIDE DERIVATIVES USEFUL FOR THE TREATMENT OF PAIN
MA27775A1 (en) ORGANIC COMPOUNDS
MA28747B1 (en) Pyridine Derivatives
TN2014000147A1 (en) (4-PHENYLIMIDAZOL-2-YL) ETHYLAMINE DERIVATIVES USEFUL AS SODIUM CHANNEL MODULATORS
MA29926B1 (en) PYRAZINE DERIVATIVES
MA31447B1 (en) NOVEL DICARBOXYLIC ACID DERIVATIVES AS S1P1 RECEPTOR AGONISTS
MA27990A1 (en) PIPERAZINE DERIVATIVES FOR THE TREATMENT OF HIV INFECTIONS
MA30403B1 (en) CYCLOALKYLAMINE ACID DERIVATIVES AND THEIR PHARMACEUTICAL COMPOSITIONS
MA31949B1 (en) Aminotriazole derivatives act as an antagonist of alx
MA51204B1 (en) Pharmaceutical forms comprising a plasma kallikrein inhibitor
MA27389A1 (en) NEW BENZIMIDAZOLE DERIVATIVES USEFUL AS ANTIPROLIFERATIVE AGENTS.
MA30232B1 (en) HYDANTOIN BASED KINASE INHIBITORS
MA30166B1 (en) SUBSTITUTED IMIDAZOLES AND THEIR USE AS PESTICIDES.
MA29170B1 (en) PURINIC DERIVATIVES AS A2A RECEPTOR AGONISTS
MA33533B1 (en) Pharmaceutical formulations for the treatment of cancer and other diseases or disorders
MA30539B1 (en) PIPERAZINYL DERIVATIVES USEFUL IN THE TREATMENT OF DISEASES INDUCED BY THE GPR38 RECEPTOR.
MA34308B1 (en) SUBSTITUTED TRIAZOLOPYRIDINES
MA49127B1 (en) N-substituted indole derivatives
MA43913A (en) POSITIVE ALLOSTERIC MODULATORS OF THE MUSCARINIC M1 RECEPTOR
MA27716A1 (en) 4-aminopyrimidine-5-ONE
MA32781B1 (en) Arecyclohexylether of dihydrotetrazapenzoazole for use as an antagonist of vasopressin receptor v1a
MA31142B1 (en) HETEROARYL DERIVATIVES OF PYRROLIDINYL AND PIPERDINYL KERONES.